Changes of phospholipase D activity in TNF-alpha and anti-Fas/Apo1 monoclonal antibody induced apoptosis in HL-60 and A20 cells

Exp Mol Med. 1998 Mar 31;30(1):21-7. doi: 10.1038/emm.1998.3.

Abstract

The changes of phospholipase D (PLD) activity were investigated during the courses of apoptotic process induced by tumor necrosis factor (TNF)-alpha or anti-Fas/Apo1 antibody in human premyelocyte HL-60 and murine B cell lymphoma A20 cells. The treatment of recombinant TNF-alpha to HL-60 cells resulted in the increased PLD activity as determined by the phosphatidylethanol formation in the presence of 1% ethanol. The enhancement of PLD activity was also observed in the anti-Fas/Apo1 monoclonal antibody-treated A20 cells. However, the activity of PLD was maximized when HL-60 and A20 cells were treated with either TNF-alpha or anti-Fas/Apo1 monoclonal antibody for 6 h. Both TNF-alpha and anti-Fas/Apo1 monoclonal antibody increased PLD activity in a dose-dependent manner up to 200 U/ml and 200 ng/ml, respectively. When the intracellular activity of protein kinase C (PKC) was interrupted by treatment of calphostin-C, both the PLD activation and the apoptosis induced by TNF-alpha and anti-Fas/Apo1 monoclonal antibody appeared to be inhibited. Since PKC is reported to activate PLD, the results indicate that the intracellular signaling cascade via PLD may play a role in the induction of apoptosis induced by TNF-alpha and anti-Fas/Apo1 monoclonal antibody.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Apoptosis*
  • DNA Fragmentation
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • HL-60 Cells
  • Humans
  • Leukemia, Promyelocytic, Acute
  • Lymphoma, B-Cell
  • Mice
  • Naphthalenes / pharmacology
  • Phospholipase D / metabolism*
  • Protein Kinase C / antagonists & inhibitors
  • Receptors, Tumor Necrosis Factor / metabolism*
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / pharmacology*
  • fas Receptor / immunology
  • fas Receptor / metabolism*

Substances

  • Antibodies, Monoclonal
  • Naphthalenes
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha
  • fas Receptor
  • Protein Kinase C
  • Phospholipase D
  • calphostin C